Johnson & Johnson Careers

MA Manager, Immunology-Beijing

Beijing, China
Medical Affairs


Job Description

Requisition ID: 1805652873W

Directs the operational function in medical affairs to achieve organizational objectives. Responsible for the design, development and implementation of programs related to educational, promotional and reporting materials for products related to Phase IIIb, Phase IV trials, solicited and non-solicited studies, publications, and so on. Manages the design and implementation plans of medical affairs program, including identification of critical paths, budget development and tracking of all projects. Manages and delegates work of direct reports. Establishes accountability for assignments. Manages creation of educational, promotional and reporting materials for use by internal stakeholders. Manages publication planning, preparation and review. Supports technical training needs of partners. Manages review of promotional material. Implements plans for clinical trials, including protocol, staffing and budgeting as it relates to business initiatives. Ensures that trials/registries are conducted according to all applicable guidelines, regulations, company procedures and high ethical/quality standards. Implements policies and procedures for development and provision of medical and technical information pertaining to the company's products for internal use by customer and by government. Manages budget, contract negotiation and oversight of vendor activities. Executes the company's drug surveillance/product safety program which includes following up on adverse reaction reports. Provides solutions surrounding legal liability and compliance with government. Maintains collaborative working relationship between medical affairs and internal stakeholders to deliver timely and expert support to product development.
Qualifications
Directs the operational function in medical affairs to achieve organizational objectives. Responsible for the design, development and implementation of programs related to educational, promotional and reporting materials for products related to Phase IIIb, Phase IV trials, solicited and non-solicited studies, publications, and so on. Manages the design and implementation plans of medical affairs program, including identification of critical paths, budget development and tracking of all projects. Manages and delegates work of direct reports. Establishes accountability for assignments. Manages creation of educational, promotional and reporting materials for use by internal stakeholders. Manages publication planning, preparation and review. Supports technical training needs of partners. Manages review of promotional material. Implements plans for clinical trials, including protocol, staffing and budgeting as it relates to business initiatives. Ensures that trials/registries are conducted according to all applicable guidelines, regulations, company procedures and high ethical/quality standards. Implements policies and procedures for development and provision of medical and technical information pertaining to the company's products for internal use by customer and by government. Manages budget, contract negotiation and oversight of vendor activities. Executes the company's drug surveillance/product safety program which includes following up on adverse reaction reports. Provides solutions surrounding legal liability and compliance with government. Maintains collaborative working relationship between medical affairs and internal stakeholders to deliver timely and expert support to product development.
Primary Location
China-Beijing-Beijing
Organization
Xian-Janssen Pharmaceutical Ltd. (7043)
Job Function
Medical Affairs
Requisition ID
1805652873W